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KONJENITAL FAKTÖR XIII EKSİKLİĞİ: BİR OLGUNUN SUNUMU

Journal Name:

  • İstanbul Tıp Fakültesi Dergisi

Publication Year:

  • 1999

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Congenital Factor XIII Defîciency: A Case Report. Congenital factor XIII (FXIII) defici-eney is a rare autosomal recessive disorder. The typical findings are neonatal umblical cord bleeding, delayed bleeding, after trauraa and surgical procedures, Lntracranial bleeding, recur-rent miscarriages in female patients and defeetive wound healing. The frequency of FXin de-ficieney in general population bas been estimated at one patient in two million. Here we pre-sent the clînical and laboratory findings of a case with FXIII deficieney.
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Abstract (Original Language): 
Konjenital Faktör XIII (FXUI) eksikliği nadir rastlanan otozomal resesif geçişli bir hastalıktır. Tipik bulguları yenidoğanda göbek kordonunda kanama, travma veya cenahı girişim sonrasında geç dönemde kanama, intrakranyal kanama, kadın hastalarda tekrarlayan düşükler vc yara iyileşmesinde gecikmedir. Genel populasyonda FXIII eksikliğinin sıklığı iki milyonda bir olarak tahmin edilmektedir. Bu yazıda FXIII eksikliği olan bir hastanın klinik ve laboratuar bulguları sunulmaktadır.
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  • 4
427-430
  • Turkish

REFERENCES

References: 

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